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WHO Drug Information Vol WHO Drug Information Vol. 30, No. 1, 2016 WHO Drug Information Contents Concept paper for comment Regulatory news 3 A framework for risk-based identification 56 Medicines regulation of essential medicine products for local New biosimilar regulations in Australia ; EMA manufacturing in low- and middle-income launches PRIME scheme for medicines countries targeting unmet needs ; EMA guidance for industry on clinical studies and clinical data publication; EMA increases access to reports Safety of medicines on adverse reactions ; Safety features on 24 The WHO Collaborating Centre for packaging to be introduced in Europe International Drug Monitoring 57 International Health Regulations 29 Look-alike sound-alike drug name confusion: Poliovirus spread : continued public health emergency; Zika virus disease a public trastuzumab emtansine health emergency 58 Blood safety FDA updates blood donor deferral policies Quality of medicines 59 Approved 35 Quality of misoprostol products Sebelipase alfa: for lysosomal acid lipase (LAL) deficiency; Selexipag : for pulmonary arterial hypertension; Albutrepenonacog alfa : for Haemophilia B ; Recombinant von Willebrand factor : for control of bleeding Prequalification episodes; Emtricitabine / tenofovir alafenamide: for HIV infection; 40 WHO rotational fellowships: an update Emtricitabine / rilpivirine / tenofovir alafenamide : for HIV infection; Elbasvir / grazoprevir : for hepatitis C virus (HCV) infection; Uridine triacetate : for emergency treatment of chemotherapy overdose ; Elotuzumab : for multiple myeloma; Alectinib : for certain advanced non-small cell lung cancers ; Lesinurad : for hyperuricaemia; Safety news Brivaracetam : for epilepsy; 46 Restrictions 61 “Follow-on” biological product Nicorandil : Use only as second-line angina treatment; Fosamprenavir : contraindicated with Insulin glargine paritaprevir; Ombitasvir / paritaprevir / ritonavir : extended contraindication; Erlotinib : only for certain types of non-small cell lung cancer; 62 Extensions of indications 47 Safety warnings Nivolumab : for kidney cancer; Eribulin : for liposarcoma; Thalidomide : reduced starting dose in patients over 75 years; Nintedanib : avoid in hepatic function disorder; Lenvatinib : tumour haemorrhage; Biphosphonates : very rare osteonecrosis of external ear canal ; Atovaquone : agranulocytosis and leukopenia; 48 Known risks Publications and events SGLT-2 inhibitors : ketoacidosis and urinary tract infections; Elvitegravir/cobicistat/ 63 Development emtricitabine/tenofovir : interactions with anticonvulsants; Nivolumab : diabetes mellitus and ketoacidosis WHO report on health development goals ; Natalizumab : new measures to manage PML; Fingolimod : new measures to minimize PML and BCC risks; Methylphenidate : 63 Access to health products hepatic failure; Varenicline : psychiatric symptoms and potential alcohol interaction; MPP signs licensing agreements ; Call for 51 Label changes applications for the 2017 WHO Model EML Posaconazole : dosing of oral formulations not interchangeable; Rosiglitazone : Risk Evaluation and Mitigation Strategy eliminated; and EMLc; Impact factor of key medicines 51 Unchanged recommendations ; Making medicines in Africa; WHO to fast- Rivaroxaban : clinical trial conclusions maintained; track availability of Zika diagnostics 52 Safety reviews 65 Diseases 52 Medicines quality Top emerging pathogens; Ebola : transmission chains stopped but new flare-ups likely ; Malaria : more countries moving towards Pharmaceuticals from Tianjin City region : potential contamination; elimination; Rabies : new global framework launched; ; Baclofen active pharmaceutical ingredient : potential 66 Antibiotics contamination; Notice of concern for Cadila Healthcare Ltd Industry declaration on combating 54 Falsified product alerts antimicrobial resistance Phenobarbitone; Yellow fever vaccines; Hepatitis C medicines Consultation documents 67 The International Pharmacopoeia 67 Misoprostol Continued Pre-publication draft - page numbers are not for citation purposes 1 WHO Drug Information Vol. 30, No. 1, 2016 Continued 72 Misoprostol dispersion International Nonproprietary 76 Misoprostol tablets Names (INN) 79 Carbamazepine 84 Carbamazepine tablets 93 Recommended INN: List 75 87 Carbamazepine chewable tablets 90 Carbamazepine oral suspension International Conference of Drug Regulatory Authorities (ICDRA) The 17th ICDRA will take place in Cape Town, South Africa 27 November – 2 December 2016 Abbreviations and web sites CHMP Committee for Medicinal Products for Human Use (EMA) EMA European Medicines Agency (www.ema.europa.eu) EU European Union FDA U.S. Food and Drug Administration (www.fda.gov) Health Canada Federal department responsible for health product regulation in Canada (www.hc-sc.gc.ca) MHLW Ministry of Health, Labour and Welfare, Japan MHRA Medicines and Healthcare Products Regulatory Agency, United Kingdom (www.mhra.gov.uk) Medsafe New Zealand Medicines and Medical Devices Safety Authority (www.medsafe.govt.nz) PRAC Pharmacovigilance Risk Assessment Committee (EMA) PMDA Pharmaceuticals and Medical Devices Agency, Japan (www.pmda.go.jp/english/index.htm) Swissmedic Swiss Agency for Therapeutic Products (www.swissmedic.ch) TGA Therapeutic Goods Administration, Australia (www.tga.gov.au) U.S. United States of America Note: The online version of this issue (available at www.who.int/medicines/publications/druginformation) has direct clickable hyperlinks to the documents and web pages referenced. 2 Pre-publication draft - page numbers are not for citation purposes WHO Drug Information Vol. 30, No. 1, 2016 Concept paper for comment A framework for risk-based identification of essential medicine products for local manufacturing in low- and middle-income countries This is the first draft of a concept paper for discussion. It aims to provide a risk assessment strategy and aspects to consider when evaluating whether an essential medicine can be manufactured locally in low- and middle-income countries with relatively limited pharmaceutical manufacturing capability and experience. This concept paper is part of the work that WHO is initiating, in collaboration with UNIDO, to promote quality local production of medicines in developing countries. The paper is intended to be developed into a joint document which provides guidance to manufacturers, regulatory officials and policy makers on how to minimize risk in manufacturing operations by selecting appropriate essential medicines for production in accordance with existing levels of GMP compliance, and how to tailor technical assistance to implement this approach, with the ultimate goal to eventually achieve local production of medicines by fully GMP-compliant manufacturers in developing countries. A second concept paper on Good Manufacturing Practice (GMP) road mapping is being prepared by UNIDO and will also be published in this journal for comments. Comments and suggestions on this paper are invited to facilitate further discussion. They should be sent to [email protected]. Introduction Background A number of papers have been published that discuss the manufacturing of medicinal products in low- and middle-income countries (LMICs) in various contexts. These include the diseases to be treated, capacity building, access to medicines, cost, skills, training, job creation, intellectual property rights, transfer of technology, government incentives, and advantages and disadvantages (e.g 1, 2, 3, 4, 5). At the African Union Conference of Ministers of Health, held in Johannesburg in April 2007 (6), a Pharmaceutical Manufacturing Plan for Africa was proposed: “This plan of action is being presented in phases to allow intense assessment of the feasibility and modality of local manufacturing of medicines in Africa.” The paper further suggested that “the plan must investigate and suggest criteria for determining what is to be produced.” One of the conclusions of this proposal stated: “Local production can be successfully done in the continent. However, there is need for the African countries to reassess the realities, possibilities and the feasibility of the programme so that it moves from being a political slogan to a reality after good ground work. The time needed to do thorough scientific analyses in the continent, together with WHO and other bodies that can add value, is certainly longer than two years.” Often an assessment of what is to be produced focuses on the diseases to be treated, with little attention to the level of technology involved with respect to the development and manufacture of pharmaceutical products in LMICs. The technology level does not only Pre-publication draft - page numbers are not for citation purposes 3 Concept paper for comment WHO Drug Information Vol. 30, No. 1, 2016 affect the feasibility of the manufacturing process, including packaging and quality control testing, but also the overall quality assurance system of the manufacturer, as well as the capacity of the local national medicines regulatory authority (NMRA) to effectively assess the resultant dossier, to conduct inspections and to regulate life cycle variations. These activities by manufacturer and NMRA are essential to ensure that the patient is getting medicines of acceptable safety, efficacy and quality, according to WHO standards as set out in WHO guidelines. It is thus appropriate to consider the level of manufacturing technology in conjunction with the risk associated with the product itself, including the ingredients and the type of manufacture when selecting products
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